Canonical Allele Identifier: CA1180934163

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837504A= , CM000663.2:g.92837504A= GRCh38
NC_000001.10:g.93303061A= , CM000663.1:g.93303061A= GRCh37
NC_000001.9:g.93075649A= NCBI36
NG_011779.1:g.10468A=
NG_033051.1:g.129019T=
NG_011779.2:g.10519A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.576A= (RPL5) MANE Select ENSP00000359345.2:p.Ala192=
ENST00000645119.1:c.324+2591A= (RPL5) ENSP00000493811.1:n.324+2591A=
ENST00000645300.1:c.426A= (RPL5) ENSP00000495589.1:p.Ala142=
ENST00000645908.1:n.310A= (RPL5)
ENST00000370321.7:c.576A= (RPL5) ENSP00000359345.2:p.Ala192=
ENST00000497519.1:n.895A= (RPL5)
ENST00000615519.4:c.475-4470T= (DIPK1A) ENSP00000483279.1:n.475-4470T=
NM_000969.3:c.576A= (RPL5) NP_000960.2:p.Ala192=
NM_001252273.1:c.475-4470T= (DIPK1A) NP_001239202.1:n.475-4470T=
NM_000969.5:c.576A= (RPL5) MANE Select NP_000960.2:p.Ala192=
NR_146333.1:n.635A= (RPL5)
NM_001252273.2:c.475-4470T= (DIPK1A) NP_001239202.1:n.475-4470T=